{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Brea",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81547",
      "recalling_firm": "Radiometer America Inc",
      "address_1": "250 S Kraemer Blvd",
      "address_2": "",
      "postal_code": "92821-6232",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was nationwide.  There was also military/government distribution.  Foreign distribution was made to Canada.",
      "recall_number": "Z-0682-2019",
      "product_description": "ABL800 analyzer, model numbers 393-800 and 393-801.",
      "product_quantity": "2,131 analyzers",
      "reason_for_recall": "The analyzer software may cause a mis-match of patient demographics and test results when a certain sequence of events occur.",
      "recall_initiation_date": "20180703",
      "center_classification_date": "20181222",
      "termination_date": "20230830",
      "report_date": "20190102",
      "code_info": "Model 393-800   ABL800 Series w/o Creatinin (All serial numbers) for the following configurations:  ABL800, ABL805, ABL810, ABL815, ABL820, ABL825, ABL830, and ABL835.    Model 393-801   ABL800 Series with Creatinin (All serial numbers) for the following configurations: ABL817, ABL827, and ABL837.",
      "more_code_info": ""
    }
  ]
}